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FDA 510(k)

MAM-3RM-A MAMMOGRAPHIC X-RAY SYSTEM

K-Number: K912974 · 1991-09-19

ApplicantElscint, Inc.
Decision Date1991-09-19
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAM-3RM-A MAMMOGRAPHIC X-RAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Elscint, Inc.. It received FDA 510(k) clearance on 1991-09-19 under 510(k) number K912974. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAM-3RM-A MAMMOGRAPHIC X-RAY SYSTEM?

MAM-3RM-A MAMMOGRAPHIC X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 1991-09-19. The listed applicant is Elscint, Inc.. The 510(k) number is K912974.

When did MAM-3RM-A MAMMOGRAPHIC X-RAY SYSTEM receive FDA 510(k) clearance?

MAM-3RM-A MAMMOGRAPHIC X-RAY SYSTEM received FDA 510(k) clearance on 1991-09-19, under 510(k) number K912974.

Who is the listed applicant for MAM-3RM-A MAMMOGRAPHIC X-RAY SYSTEM?

The FDA 510(k) record lists Elscint, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAM-3RM-A MAMMOGRAPHIC X-RAY SYSTEM?

The FDA product code for MAM-3RM-A MAMMOGRAPHIC X-RAY SYSTEM is IZH.

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Other records listing Elscint, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K983313ADVANCED AUTOMATIC DETECTOR SELECTION OPTION FOR GLORYK982060VOLUMAX CT IMAGING SYSTEMK974344CT SCOPEK980306GYREX 2T PRESTIGE, GYREX PRIMA ITG, GYREX PRIVILEGE, GYREX V-EPK974614GYREX 2T PRESTIGE 100-6321-0107, GYREX PRIVILEDGE 100-6326-0102, GYREX PRIMA 1TG 100-6250-0102K9725922T PRESTIGE(100-6321-0107)/PRIVILEGE(100-6326-0102)/GYREX V-EP(100-6327-0101)

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Related Devices (Code: IZH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K203509SMART FINDERIms Giotto S.P.A.K202294Affirm Contrast BiopsyHologic, Inc.K191495Biopsy PositionerFujifilm CorporationK161575Affirm Lateral Arm Upright Biopsy AccessoryHologicK161920Comfort CoverPrecision Dynamics CorporationK153486Affirm Prone Biopsy SystemHologic, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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